Clearance Summary
Renovo Life Small Bone IM Nail System received FDA 510(k) clearance under submission number K161254, sponsored by Renovo Life, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-11-07.
- Submission: K161254
- Applicant / Sponsor: Renovo Life, LLC
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3020
- Decision date: 2016-11-07
Classification & Regulation
This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.